Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

W Timothy O'Brien

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Molecular Endocrinology (Baltimore, Md.)|February 21, 2014
Behavioral changes and dopaminergic dysregulation in mice lacking the nuclear receptor Rev-erbαJennifer Jager, W Timothy O'Brien, Jessica Manlove, et al.
Frontiers in Behavioral Neuroscience|October 24, 2014
An open-source toolbox for automated phenotyping of mice in behavioral tasksTapan P Patel, David M Gullotti, Pepe Hernandez, et al.
Current Biology : CB|October 15, 2021
The dihydropyrimidine dehydrogenase gene contributes to heritable differences in sleep in miceBrendan T Keenan, Raymond J Galante, Jie Lian, et al.
American Journal of Medical Genetics. Part A|June 24, 2023
Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and miceDivya Nair, Abdias Diaz-Rosado, Elisa Varella-Branco, et al.
Neurobiology of Learning and Memory|January 9, 2018
Rigor and reproducibility in rodent behavioral researchMaria Gulinello, Heather A Mitchell, Qiang Chang, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
A novel mouse model of rare neurodevelopmental disorder, TBCK SyndromeAshley J Melendez-Perez, Emily L Durham, Dana E Layo-Carris, et al.
Brain : a Journal of Neurology|April 16, 2020
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of functionMonica Zilmer, Andrew C Edmondson, Sumeet A Khetarpal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 23, 2023
Dominant-negative variants in CBX1 cause a neurodevelopmental disorderYukiko Kuroda, Aiko Iwata-Otsubo, Kerith-Rae Dias, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Molecular Endocrinology (Baltimore, Md.)|February 21, 2014
Behavioral changes and dopaminergic dysregulation in mice lacking the nuclear receptor Rev-erbαJennifer Jager, W Timothy O'Brien, Jessica Manlove, et al.
Frontiers in Behavioral Neuroscience|October 24, 2014
An open-source toolbox for automated phenotyping of mice in behavioral tasksTapan P Patel, David M Gullotti, Pepe Hernandez, et al.
Current Biology : CB|October 15, 2021
The dihydropyrimidine dehydrogenase gene contributes to heritable differences in sleep in miceBrendan T Keenan, Raymond J Galante, Jie Lian, et al.
American Journal of Medical Genetics. Part A|June 24, 2023
Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and miceDivya Nair, Abdias Diaz-Rosado, Elisa Varella-Branco, et al.
Neurobiology of Learning and Memory|January 9, 2018
Rigor and reproducibility in rodent behavioral researchMaria Gulinello, Heather A Mitchell, Qiang Chang, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
A novel mouse model of rare neurodevelopmental disorder, TBCK SyndromeAshley J Melendez-Perez, Emily L Durham, Dana E Layo-Carris, et al.
Brain : a Journal of Neurology|April 16, 2020
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of functionMonica Zilmer, Andrew C Edmondson, Sumeet A Khetarpal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 23, 2023
Dominant-negative variants in CBX1 cause a neurodevelopmental disorderYukiko Kuroda, Aiko Iwata-Otsubo, Kerith-Rae Dias, et al.
Pageof 2